Endo Is Not The End

Taylor is a 24-year-old young professional living with endometriosis, heart arrhythmias, pelvic floor dysfunction, sleep apnea, and severe allergies. Working in politics and government, she uses her lived experience to connect with others and advocate for healthcare policy and women’s rights.

Saturday, May 23, 2020

What I’ve Been Watching

›

I’m the type of person that needs a lot of alone time to relax and unwind and I like to do that by watching TV shows. It helps me escape fro...

Saturday, May 9, 2020

Good Things About Quarantining with Endometriosis

›

This may be an unpopular opinion, but quarantining with Endometriosis is not that bad. Having a chronic disease makes you miss out on a lot ...

Saturday, April 25, 2020

My Favorite Endometriosis Bloggers

›

Today I wanted to share my favorite Endometriosis bloggers with you so you all can see the women I look up to in this crazy world of Endomet...

Saturday, April 11, 2020

Immunocompromised During COVID-19

›

This pandemic is a scary time in the world for everyone, but please take a second to think about those who are immunocompromised, like peopl...

Saturday, March 28, 2020

Day in My Life

›

Today I wanted to share a day in my life. I think a lot of people wonder what life is like living with a chronic illness. Well, my life is p...

Saturday, March 14, 2020

Easy Exercise Routine for Chronic Pain

›

Exercising is always something I have struggled with. I always get in a good routine, then have a flare-up and stop going to the gym. Recent...

Saturday, March 7, 2020

Myths and Misconceptions

›

Myth: Endometriosis is just a really heavy period. Women with Endo may experience a really heavy period, but that is just one of the many s...

‹

›

Home

View web version

About Me

Taylor Sprague: Taylor is a 24-year-old young professional navigating life with multiple chronic health conditions, including endometriosis, heart arrhythmias, pelvic floor dysfunction, sleep apnea, and severe allergies. Through her lived experience, she uses this space to connect with others facing similar challenges and to educate readers about chronic illness, self-advocacy, and the realities of living in a body that doesn’t always cooperate. Professionally, Taylor works in politics and government, where she is a strong advocate for accessible, equitable healthcare policy and women’s rights. This blog sits at the intersection of personal storytelling and public policy, blending vulnerability with advocacy in the hope that no one feels alone in their diagnosis, and that lived experiences help drive meaningful change.

View my complete profile